Package 21130-056-80

Brand: ibuprofen pm

Generic: diphenhydramine citrate, ibuprofen
NDC Package

Package Facts

Identity

Package NDC 21130-056-80
Digits Only 2113005680
Product NDC 21130-056
Description

1 BOTTLE, PLASTIC in 1 BOX (21130-056-80) / 80 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-12-31
Brand ibuprofen pm
Generic diphenhydramine citrate, ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "792e598a-eaee-4d0a-9c99-154ecbf29aaf", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0321130777564"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["e49d1e9e-99a6-4d81-90d6-ef23a584a3d1"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Safeway, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (21130-056-40)  / 40 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-056-40", "marketing_end_date": "20261231", "marketing_start_date": "20240301"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (21130-056-80)  / 80 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-056-80", "marketing_end_date": "20261231", "marketing_start_date": "20240301"}], "brand_name": "Ibuprofen PM", "product_id": "21130-056_792e598a-eaee-4d0a-9c99-154ecbf29aaf", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-056", "generic_name": "Diphenhydramine Citrate, Ibuprofen", "labeler_name": "Safeway, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen PM", "active_ingredients": [{"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA211404", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20240301"}